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Wieacker Syndrome

Abstract

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NORD is very grateful to Dr. Annick Toutain from the Service de Genetique Hopital Bretonneau, Tours, France, for assistance in the preparation of this report.

Synonyms of Wieacker Syndrome

Apraxia, Oculomotor, with Congenital Contractures and Muscle Atrophy
Contractures of Feet, Muscle Atrophy, and Oculomotor Apraxia
Wieacker-Wolff Syndrome
WWS

Disorder Subdivisions

No subdivisions found.

General Discussion

Wieacker syndrome is a rare, slowly progressive, genetic disorder characterized by deformities of the joints of the feet (contracture), muscle degeneration (atrophy), mild mental retardation and an impaired ability to move certain muscles of the eyes, face and tongue. Wieacker syndrome is inherited as an X-linked recessive trait.

Organizations related to Wieacker Syndrome

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